Min Cho

PolyDADMAC and Dimethylamine as Precursors of N-Nitrosodimethylamine during Ozonation: Reaction Kinetics and Mechanisms

Interactions of ozone with organic precursors during water treatment may generate carcinogenic N-nitrosodimethylamine (NDMA) byproduct. This study investigates the reaction mechanisms responsible for NDMA formation from ozonation of the commonly used poly(diallyldimethylammonium chloride) (polyDADMAC) coagulant. Upon ozonation, polyDADMAC yields the highest amount of NDMA among several water treatment polymers, including polyamines and cationic polyacrylamides. Ozonation transforms polyDADMAC to dimethylamine (DMA) and NDMA formation is correlated to polyDADMAC degradation and DMA release. Hydroxyl radicals generated from ozone play an important role in the degradation of polyDADMACs quaternary ammonium ring groups and subsequent release of secondary amine. Although nitrite and formaldehyde are detected as ozonation products of DMA and polyDADMAC, contribution of formaldehyde-enhanced nitrosation pathway is determined to be insignificant in NDMA formation. In contrast, reaction of hydroxylamine, another ozonation product of DMA, with DMA in the presence of ozone is deemed critical in the formation of NDMA during ozonation. The study results show that that contact of polyDADMAC with ozone will lead to release of the more potent NDMA precursor DMA but may not generate a significant amount of NDMA under typical drinking water treatment conditions due to low yield. The mechanistic understanding from this study can help develop source control strategies for minimization of NDMA formation risk at water and wastewater utilities.

Characterization of lead resistant endophytic Bacillus sp. MN3-4 and its potential for promoting lead accumulation in metal hyperaccumulator Alnus firma

The aim of this study was to isolate and characterize endophytic bacteria from the roots of the metal hyperaccumulator plant Alnus firma. A total of 14 bacterial endophytes were isolated from root samples and assayed for tolerance to heavy metals. Isolate MN3-4 exhibited maximum bioremoval of Pb and was subsequently identified as Bacillus sp. based on 16S rRNA sequences. The pH and initial metal concentration highly influenced the Pb bioremoval rate. The growth of isolate MN3-4 was moderately altered in the presence of metals. Scanning electron microscopy, energy dispersive spectroscopy, biological-transmission electron microscopy, and Fourier transform infrared spectroscopy studies revealed that isolate MN3-4 had extracellularly sequestered the Pb molecules with little intracellular accumulation. Isolate MN3-4 did not harbor pbrA and pbrT genes. Moreover, isolate MN3-4 had the capacity to produce siderophores and indoleacetic acid. A root elongation assay demonstrated an increase (46.25%) in the root elongation of inoculated Brassica napus seedlings compared to that of the control plants. Obtained results pointed out that isolate MN3-4 could potentially reduce heavy metal phytotoxicity and increase Pb accumulation in A. firma plants.

Green synthesis of silver and gold nanoparticles using Zingiber officinale root extract and antibacterial activity of silver nanoparticles against food pathogens

AbstractnIn the present study, we synthesized silver and gold nanoparticles with a particle size of 10–20xa0nm, using Zingiber officinale root extract as a reducing and capping agent. Chloroauric acid (HAuCl4) and silver nitrate (AgNO3) were mixed with Z. officinale root extract for the production of silver (AgNPs) and gold nanoparticles (AuNPs). The surface plasmon absorbance spectra of AgNPs and AuNPs were observed at 436–531xa0nm, respectively. Optimum nanoparticle production was achieved at pH 8 and 9, 1xa0mM metal ion, a reaction temperature 50xa0°C and reaction time of 150–180xa0min for AgNPs and AuNPs, respectively. An energy-dispersive X-ray spectroscopy (SEM–EDS) study provides proof for the purity of AgNPs and AuNPs. Transmission electron microscopy images show the diameter of well-dispersed AgNPs (10–20xa0nm) and AuNPs (5–20xa0nm). The nanocrystalline phase of Ag and Au with FCC crystal structures have been confirmed by X-ray diffraction analysis. Fourier transform infrared spectroscopy analysis shows the respective peaks for the potential biomolecules in the ginger rhizome extract, which are responsible for the reduction in metal ions and synthesized AgNPs and AuNPs. In addition, the synthesized AgNPs showed a moderate antibacterial activity against bacterial food pathogens.

Laccase-poly(lactic-co-glycolic acid) (PLGA) nanofiber: Highly stable, reusable, and efficacious for the transformation of diclofenac

Nanobiocatalysis has received growing attention for use in commercial applications. We investigated the efficiency, stability, and reusability of laccase-poly(lactic-co-glycolic acid) (PLGA) nanofiber for diclofenac transformation. NH stretching vibrations (3400-3500 cm(-1) and 1560 cm(-1)) in FT-IR spectra confirmed immobilization of laccase on PLGA nanofibers. The relative activity of immobilized laccase was 82% that of free laccase. Immobilized laccase had better storage, pH, and thermal stability than free laccase. The immobilized laccase produced complete diclofenac transformation in three reuse cycles, which was extended to 6 cycles in the presence of syringaldehyde. Results suggest that laccase-PLGA nanofiber may be useful for removing diclofenac from aqueous sources and has potential for other commercial applications.

C60 Aminofullerene Immobilized on Silica as a Visible-Light-Activated Photocatalyst

A new strategy is described to immobilize photoactive C(60) aminofullerene on silica gel (3-(2-succinic anhydride)propyl functionalized silica), thus enabling facile separation of the photocatalyst for recycling and repeated use. An organic linker moiety containing an amide group was used to anchor C(60) aminofullerene to the functionalized silica support. The linker moiety prevents aqueous C(60) aggregation/agglomeration (shown by TEM images), resulting in a remarkable enhancement of photochemical (1)O(2) production under visible light irradiation. With no loss in efficacy of (1)O(2) production plus insignificant chemical modification of the aminoC(60)/silica photocatalyst after multiple cycling, the system offers a promising new visible-light-activated photocatalyst. Under visible-light irradiation, the aminoC(60)/silica photocatalyst is capable of effective and kinetically enhanced oxidation of Ranitidine and Cimetidine (pharmaceutical pollutants) and inactivation of MS-2 bacteriophage compared to aqueous solutions of the C(60) aminofullerene alone. Thus, this photocatalyst could enable water treatment in less developed areas by alleviating dependence on major infrastructure, including the need for electricity.

Significance of autochthonous Bacillus sp. KK1 on biomineralization of lead in mine tailings.

The aim of the study was to isolate and characterize potential autochthonous bacteria for biomineralization of Pb in mine tailings. A total of four bacteria were isolated from the soil samples and assayed for tolerance to Pb and other heavy metals. Isolate KK1 exhibited maximum Pb resistance and was subsequently identified as Bacillus sp. based on the partial 16S rRNA gene sequences. The isolate KK1 reduced the Pb ions and did not harbor pbrT gene. Selective sequential extraction of bioaugmented soil revealed that the isolate significantly reduced (26%) the exchangeable fraction and increased (38%) the carbonate fraction of Pb. X-ray diffraction studies confirmed the role of bacterially induced calcite precipitation in the bioremediation of mine tailings. A significant increase in the urease (334%), DHO (dehydrogenase) (14%), and phosphatase (37%) activity was observed in the bioaugmented mine soil.

Converting Visible Light into UVC: Microbial Inactivation by Pr3+-Activated Upconversion Materials

Herein we report the synthesis and properties of light-activated antimicrobial surfaces composed of lanthanide-doped upconversion luminescent nano- and microcrystalline Y(2)SiO(5). Unlike photocatalytic surfaces, which convert light energy into reactive chemical species, this work describes surfaces that inactivate microorganisms through purely optical mechanisms, wherein incident visible light is partially converted into germicidal UVC radiation. Upconversion phosphors utilizing a Pr(3+) activator ion were synthesized and their visible-to-ultraviolet conversion capabilities were confirmed via photoluminescence spectroscopy. Polycrystalline films were prepared on glass substrates, and the extent of surface microbial inactivation and biofilm inhibition under visible light excitation were investigated. Results show that, under normal visible fluorescent lamp exposure, a sufficient amount of UVC radiation was emitted to inhibit Pseudomonas aeruginosa biofilm formation and to inactivate Bacillus subtilis spores on the dry surfaces. This new application of upconversion luminescence shows for the first time its ability to deter microbial contamination and could potentially lead to new material strategies for disinfection of surfaces and water.

Antimicrobial fabrication of cotton fabric and leather using green-synthesized nanosilver

This study aims to investigate the green synthesis of silver nanoparticles (AgNPs) by Erigeron annuus (L.) pers flower extract as reducing and capping agent, and evaluation of their antibacterial activities for the first time. The obtained product was confirmed by UV-Vis spectrum, high resolution-transmission electron microscopy, energy-dispersive X-ray spectroscopy, Fourier transform infrared spectroscopy, and X-ray diffraction studies. The optimum AgNPs production was achieved at pH 7, metal silver (Ag(+) ion) concentration of 2.0mM, flower extract concentration 4%, and time 335 min. In addition, the antibacterial activity of cotton fabrics and tanned leather loaded with AgNPs, commercial AgNPs, flower extract, Ag(+) ion and blend of flower extract with AgNPs were evaluated against Gram-positive odor causing bacteria Brevibacterium linens and Staphylococcus epidermidis. The results showed maximum zone of inhibition (ZOI) by the cotton fabrics embedded with blend of flower extract and AgNPs against B. linens. The structure and morphology of cotton fabric and leather samples embedded with AgNPs, Ag(+) ion and blend of flower extract with AgNPs were examined under field emission scanning electron microscope.

Visible light sensitized inactivation of MS-2 bacteriophage by a cationic amine-functionalized C60 derivative.

Recently, we reported the successful synthesis of various hexakis C60 derivatives (i.e., C60 with six functional groups containing NH3+-, CO2H-, or OH-terminals) with enhanced stability in water for aqueous phase application (Lee et al., Environ. Sci. Technol. 2009, 43, pp 6604-6610). Among these newly synthesized C60 derivatives, the cationic hexakis C60 derivative with amine functionality, C60(CR2)6 (R=CO2(CH2)2NH3+CF3CO2-), was found to exhibit remarkable efficiency to inactivate Escherichia coli and MS-2 bacteriophage under UVA irradiation. Herein, we report that this amine-functionalized C60 derivative is also photoactive in response to visible light from both commercial fluorescence lamps and sunlight. Efficient production of 1O2, facile reaction of 1O2 with proteins in MS-2 phage capsid and electrostatic attraction between positively charged C60 derivative and negatively charged MS-2 phage collectively contributed to high efficiency of MS-2 phage inactivation in this photocatalytic disinfection system. The rate of 1O2 production was evaluated using a probe compound, furfuryl alcohol, and 1O2 CT (the product of 1O2 concentration and exposure time) required to achieve a target level of virus inactivation was quantitatively analyzed. The unique visible-light sensitized virucidal property makes this C60 derivative highly desirable for the development of sustainable disinfection strategies that do not require continuous chemical addition nor an external energy source other than ambient light.

Fabrication of a ternary CdS/ZnIn2S4/TiO2 heterojunction for enhancing photoelectrochemical performance: effect of cascading electron–hole transfer

A novel, three-dimensional, ternary CdS/ZnIn2S4/TiO2 heterojunction has been fabricated via a three-step facile hydrothermal method. In this structure, one-dimensional TiO2 nanorods were directly grown on conductive fluorine-doped tin oxide (FTO) substrates. Next, to form a ternary heterojunction of CdS/ZnIn2S4/TiO2, ZnIn2S4 nanosheets were designed on the TiO2 nanorods and sensitized by CdS nanograins. A systematic photoelectrochemical study shows that the photocurrent density of the ternary heterojunction architecture is as high as 1.4 mA cm−2 at a potential of 0.1 V versus Ag/AgCl (under optimized conditions). A more detailed study shows that the photocurrent density is more than two times higher than that of a single CdS/TiO2 heterojunction (0.615 mA cm−2) and three times higher than that of ZnIn2S4/TiO2 (at 0.1 V vs. Ag/AgCl). This excellent photoelectrochemical performance is ascribed to the way that the band structure of TiO2 nanorods synergistically cascades with ZnIn2S4 and CdS, which allows for the absorption of a wider portion of the solar spectrum and improves the effective separation of the generated electron–hole pairs. Electrochemical impedance spectroscopy (EIS) studies also reveal the significant changes in both the interface resistance and the charge transfer resistance of the CdS/ZnIn2S4/TiO2 heterostructure. This can be attributed to the efficient hierarchical cascading that occurs during the electron–hole transfer from the excited CdS to TiO2 through the enlarged interface of ZnIn2S4 upon visible light illumination.